meddevicedb.com FDA Device Reference

SURGEON'S GLOVE, POWDER FREE

K052030 Class I Traditional
Decision Date
2005-09-13
Sponsor / Applicant
Shun Thai Rubber Gloves Industry Public Co., Ltd.

Technical Specification

510(k) Submission ID K052030
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2005-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGEON'S GLOVE, POWDER FREE received FDA 510(k) clearance under submission number K052030, sponsored by Shun Thai Rubber Gloves Industry Public Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2005-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.